Canonical Allele Identifier: CA508211892

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411663G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908407G>C , CM000681.2:g.50908407G>C	GRCh38
NC_000019.9:g.51411663G>C , CM000681.1:g.51411663G>C	GRCh37
NC_000019.8:g.56103475G>C	NCBI36
NG_012154.2:g.7332C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.564C>G MANE Select	ENSP00000326159.1:p.Pro188=
ENST00000324041.5:c.564C>G	ENSP00000326159.1:p.Pro188=
ENST00000431178.2:c.328+172C>G	ENSP00000399448.2:n.328+172C>G
ENST00000593885.1:c.*59C>G	ENSP00000469769.1:n.*59C>G
ENST00000596876.1:n.566C>G
ENST00000598305.5:c.*59C>G	ENSP00000469963.1:n.*59C>G
ENST00000599865.5:n.500C>G
ENST00000602148.1:c.576C>G	ENSP00000472091.1:n.576C>G
NM_001302961.1:c.279C>G	NP_001289890.1:p.Pro93=
NM_004917.4:c.564C>G	NP_004908.4:p.Pro188=
NR_126566.1:n.553C>G
XM_005259441.3:c.279C>G	XP_005259498.2:p.Pro93=
XM_011527545.1:c.*59C>G	XP_011525847.1:n.*59C>G
XM_011527546.1:c.475+172C>G	XP_011525848.1:n.475+172C>G
XM_011527547.1:c.417C>G	XP_011525849.1:p.Pro139=
XM_005259441.4:c.279C>G	XP_005259498.2:p.Pro93=
XM_011527545.3:c.*59C>G	XP_011525847.1:n.*59C>G
XM_011527546.2:c.475+172C>G	XP_011525848.1:n.475+172C>G
NM_001302961.2:c.279C>G	NP_001289890.1:p.Pro93=
NR_126566.2:n.553C>G
NM_004917.5:c.564C>G MANE Select	NP_004908.4:p.Pro188=